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Cutibacterium Acnes in Deep Tissues in Primary Spine and Shoulder Surgery

NCT05355844 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2022-05-02

No results posted yet for this study

Summary

Obtain deep tissue samples from patients undergoing primary prosthetic surgery of the shoulder and patients undergoing primary instrumented surgery of the spine. Patients will be randomized to receive benzoyl peroxide 3 days prior to surgery.

Conditions

  • Rotator Cuff Tear Arthropathy
  • Spine Degeneration

Interventions

DRUG

Benzoyl peroxide

Benzoyl peroxide application in the incision area before surgery

Sponsors & Collaborators

  • Hospital del Mar

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-31
Primary Completion
2023-05-31
Completion
2023-11-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05355844 on ClinicalTrials.gov